Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

This publication has 33 references indexed in Scilit:

• Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
  The Lancet, 2001
• An Animal Model for the Molecular Genetics of CADASIL
  Stroke, 2001
• Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3v EGF-like repeat domains
  European Journal of Human Genetics, 2000
• CADASIL: Notch signaling defect or protein accumulation problem?
  Journal of Clinical Investigation, 2000
• The Natural History of CADASIL
  Stroke, 1999
• Notch Signaling: Cell Fate Control and Signal Integration in Development
  Science, 1999
• Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
  Nature, 1996
• Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
  Acta Neuropathologica, 1995
• Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL.
  Stroke, 1994
• Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.
  Stroke, 1993